Author:
Jamzad Shahla,Fassihi Reza
Publisher
Springer Science and Business Media LLC
Subject
Drug Discovery,Pharmaceutical Science,Agronomy and Crop Science,Ecology,Aquatic Science,General Medicine,Ecology, Evolution, Behavior and Systematics
Reference22 articles.
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3. Food and Drug Administration (FDA) Center for Drug Evaluation and Research (CDER). Guidance for Industry. Modified Release Solid Oral Dosage Forms: Scale up and Post Approval Changes (SUPAC): Chemistry, Manufacturing and Controls, In Vitro Dissolution Testing and In Vivo Bioequivalence Documentation. Rockville, MD: FDA; 1997.
4. Shah VP, Konecny JJ, Everett RL, McCullough B, Noorizadeh AC, Skelly JP. In vitro dissolution profile of water-insoluble drug dosage forms in the presence of surfactants. Pharm Res. 1989;6:612–618.
5. Abdou HM. Dissolution, Bioavailability, and Bioequivalence. Easton, PA: Mack; 1989.
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127 articles.
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